Németh K, Holics K, Ujhelyi R, Váradi A, Fekete G
II. Sz. Gyermekklinika, Semmelweis Orvostudományi Egyetem Budapest.
Orv Hetil. 1996 Apr 28;137(17):899-903.
The authors screened 374 patients clinically diagnosed be affected by cystic fibrosis. Mutations delta F508, G542X, G551D, R553X, N1303K were analysed to obtain genetic diagnosis. The large number of patients involved in this study allowed for authors to present precise data of the frequencies of these mutations in Hungary. The frequency of mutation delta F508 is found to be significantly less then the numbers reported in other studies. This is due to sampling bias occurring at little sample sizes. Mutational analysis has been used as a tool of prenatal diagnosis.
作者对374例临床诊断为患有囊性纤维化的患者进行了筛查。分析了ΔF508、G542X、G551D、R553X、N1303K突变以进行基因诊断。这项研究涉及的大量患者使作者能够提供这些突变在匈牙利的精确频率数据。发现ΔF508突变的频率明显低于其他研究报告的数字。这是由于小样本量时出现的抽样偏差。突变分析已被用作产前诊断的工具。